Evidence map›Paper›PMID 32645977›Full record

ReviewCancers2020

Advances in Anti-Cancer Immunotherapy: Car-T Cell, Checkpoint Inhibitors, Dendritic Cell Vaccines, and Oncolytic Viruses, and Emerging Cellular and Molecular Targets.

Emilie Alard, Aura-Bianca Butnariu, Marta Grillo, Charlotte Kirkham, Dmitry Aleksandrovich Zinovkin, Louise Newnham, Jenna Macciochi, Md Zahidul Islam Pranjol

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  7. Review
  8. Spatio-Temporal Dynamics of MBulletin of mathematical biology · 2025
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  9. Review
  10. Lignin-Based Nanocarrier for Simultaneous Delivery ofPharmaceuticals (Basel, Switzerland) · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Personalizing Oncolytic Immunovirotherapy Approaches.Molecular diagnosis & therapy · 2024
    Article
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Emilie AlardSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.ORCID 0000-0002-7804-4121
Aura-Bianca ButnariuSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.
Marta GrilloSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.
Charlotte KirkhamSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.
Dmitry Aleksandrovich ZinovkinDepartment of Pathology, Gomel State Medical University, Gomel Region 246000, Belarus.
Louise NewnhamSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.
Jenna MacciochiSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.
Md Zahidul Islam PranjolSchool of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QG, UK.ORCID 0000-0002-6164-6281
University of Sussex · GBGomel State Medical University · BY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Unlike traditional cancer therapies, such as surgery, radiation and chemotherapy that are typically non-specific, cancer immunotherapy harnesses the high specificity of a patient's own immune system to selectively kill cancer cells. The immune system is the body's main cancer surveillance system, but cancers may evade destruction thanks to various immune-suppressing mechanisms. We therefore need to deploy various immunotherapy-based strategies to help bolster the anti-tumour immune responses. These include engineering T cells to express chimeric antigen receptors (CARs) to specifically recognise tumour neoantigens, inactivating immune checkpoints, oncolytic viruses and dendritic cell (DC) vaccines, which have all shown clinical benefit in certain cancers. However, treatment efficacy remains poor due to drug-induced adverse events and immunosuppressive tendencies of the tumour microenvironment. Recent preclinical studies have unveiled novel therapies such as anti-cathepsin antibodies, galectin-1 blockade and anti-OX40 agonistic antibodies, which may be utilised as adjuvant therapies to modulate the tumour microenvironment and permit more ferocious anti-tumour immune response.

Indexed as

CAR-T cellcathepsin Dcheckpoint inhibitordendritic cell vaccinesdrug resistancegalectin-1immunosuppressiononcolytic virusesOX40tumour-induced immune evasion

Identifiers

PMID32645977
PMCPMC7408985
OpenAlexW3040083476

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.